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Updated: Mar 26, 2026

Conducting Multiple Imaging Modes with One Fluorescence Microscope
Published on: October 28, 2018
CINCH (confocal incoherent correlation holography) super resolution fluorescence microscopy based upon FINCH (Fresnel
Nisan Siegel1, Brian Storrie2, Marc Bruce3
1Department of Biomedical Engineering, Johns Hopkins University, 9605 Medical Center Drive, Rockville, MD 20850 USA; Microscopy Center, Johns Hopkins University Montgomery County Campus, Rockville, MD 20850 USA.
Abstract:
FINCH holographic fluorescence microscopy creates high resolution super-resolved images with enhanced depth of focus. The simple addition of a real-time Nipkow disk confocal image scanner in a conjugate plane of this incoherent holographic system is shown to reduce the depth of focus, and the combination of both techniques provides a simple way to enhance the axial resolution of FINCH in a combined method called "CINCH". An important feature of the combined system allows for the simultaneous real-time image capture of widefield and holographic images or confocal and confocal holographic images for ready comparison of each method on the exact same field of view. Additional GPU based complex deconvolution processing of the images further enhances resolution.
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